Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Arda Arduç

9PUBLICATIONS
5CO-AUTHORS
Developmental genetics (incl. sex determination)NeonatologyFoetal development and medicinePsychosocial aspects of childbirth and perinatal mental healthEpigenetics (incl. genome methylation and epigenomics)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (9)

Sort by Publication Date:
|Dec 16, 2025
Can Prenatal Ultrasound and Genetic Testing Reliably Exclude Non-Isolated Clubfoot?

Jana M de Vries, Arda Arduc, Elisabeth van Leeuwen

|Nov 24, 2025
FAM20B Related Skeletal Dysplasia: Expanding the Prenatal Phenotype.

Arda Arduç, Linda C Zuurbier, Merel C van Maarle

|Nov 21, 2025
Genetic analysis in fetuses with isolated clubfoot: diagnostic insights and added value.

Jana M de Vries, Arda Arduç, Quinten Waisfisz

|Sep 06, 2025
A Practical Prenatal Ultrasound Classification System for Lower Limb Anomalies-PRELLIM Classification.

Arda Arduç, Margriet H M van Doesburg, Melinda M E H Witbreuk

|Sep 02, 2025
The Influence of the Introduction of Fetal Anomaly Scans on Pregnancy Terminations in Cases of Upper Limb Anomalies: A Retrospective Cohort Study From 2000 to 2023.

Arda Arduç, Eline Huiberts, Margriet H M van Doesburg

|Jul 27, 2025
Arthrogryposis Multiplex Congenita (AMC) and counselling before and during pregnancy: a questionnaire study.

Arda Arduç, Julia Slootbeek, Johanna I P de Vries

Pageof 2

Frequent Collaborators

4 joint publications

Ingeborg H Linskens

2 joint publications

Maria B Tan-Sindhunata

2 joint publications

Elisabeth van Leeuwen

2 joint publications

Jana M de Vries

1 joint publications

Brigitte Hw Faas

Frequent Collaborators

4 joint publications

Ingeborg H Linskens

2 joint publications

Maria B Tan-Sindhunata

2 joint publications

Elisabeth van Leeuwen

2 joint publications

Jana M de Vries

Top Related Videos

Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform
09:30

Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform

Published on : Aug 17, 2022

3.5K
In Vivo Functional Study of Disease-associated Rare Human Variants Using <em>Drosophila</em>
06:41

In Vivo Functional Study of Disease-associated Rare Human Variants Using <em>Drosophila</em>

Published on : Aug 20, 2019

14.2K
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on : Dec 01, 2017

9.0K
See more related videos

Top Related Videos

Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform
09:30

Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform

Published on : Aug 17, 2022

3.5K
In Vivo Functional Study of Disease-associated Rare Human Variants Using <em>Drosophila</em>
06:41

In Vivo Functional Study of Disease-associated Rare Human Variants Using <em>Drosophila</em>

Published on : Aug 20, 2019

14.2K
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on : Dec 01, 2017

9.0K
See more related videos